System Design Analyst II-Clinical Systems- HYBRID

Allergan; Florham Park (NJ); On-site; USD 120,000 - 180,000; Full time

Job summary

AbbVie Data Science is seeking a seasoned professional to lead and deliver complex clinical data systems in support of the Clinical Data Strategy Organization. You will drive study builds, ensure regulatory compliance, and collaborate with cross-functional teams.

The role requires extensive hands-on EDC experience (Medidata RAVE, Veeva EDC), strong CDASH/SDTM knowledge, and mentoring capabilities in a fast-paced environment within the AbbVie ecosystem.

Qualifications

• Bachelor’s degree required; Masters preferred.
• 5+ years hands-on technical study build in EDC.
• Experience with Medidata RAVE and Veeva EDC is valuable.
• In-depth knowledge of clinical trial processes (CDASH/SDTM).
• Proven ability to influence and mentor in a matrixed environment.
• Strong communication and analytical skills.

Responsibilities

• Actively participates in developing data standards and ensures designs meet protocol requirements.
• Establishes and maintains study design methodology for clinical systems.
• Ensures consistency across TA and program-level designs.
• Leads on-time design and delivery of new clinical systems and integrations.
• Interacts with CDO and cross-functional teams to align objectives.
• Adheres to GCPs and regulatory requirements and maintains quality standards.
• Coaches and mentors team members and drives innovation.
• Leads process improvement initiatives in the organization.

Skills

5+ years EDC

Medidata RAVE

Veeva EDC

CDASH

SDTM

Communication skills

Mentoring

Education

Bachelor’s degree in business/MIS/CS/life sciences

Tools

Medidata RAVE

Veeva EDC

Job description

Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

Purpose

AbbVie Data Science is the best-in-class team within its cross-industry peer group and is responsible for bringing people, process, and technology together to generate business value from clinical trials data. Our operational model is exemplified through execution and innovation. This role is key to ensuring successful delivery against the program- and study-level accountabilities assigned to Clinical Data Strategy Organization.

Responsibilities

• Actively participates in the development of common data standards and ensures systems designs comply with the standards, as well as with associated protocol requirements. Ensures that the design team utilizes standards
• Establishes and maintains methodology used by the team to design and develop clinical trial systems, benchmarking against industry standards. Ensures that systems are specified to optimize functionality, end user experience, and data flow. Ensures that the design team meets these expectations
• Ensures that TA- and program-level consistency is achieved by the design team
• Accountable for the on-time design and delivery of new clinical systems, integrations between systems, as well as any required changes to clinical systems (e.g., EDC, IRT, ePRO). Utilizes project management tools to track study progress and plan work. Anticipates and identifies issues that could affect timelines or quality and develops options and solutions
• Interacts with and influences CDO and cross-functional team members to achieve program and study objectives. Ensures that assigned work product is synchronized with upstream and downstream dependencies
• Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and functional quality standards. Stays abreast of new and/or evolving local regulations, guidelines and policies related to clinical development
• Responsible for coaching and mentoring members of the team, as well as contributes to their skill development
• Leads CDO and cross-functional innovation and process improvement initiatives

Qualifications

• Bachelor’s degree in business, management information systems, computer science, life sciences or equivalent. Masters preferred.
• Must have 5+ years of hands‑on technical Study build in EDC. Experience with technical study build in Medidata RAVE is required. Veeva EDC technical study build experience is a plus.
• In‑depth knowledge of clinical trial processes.
• In‑depth knowledge of CDASH (Required) and SDTM.
• Demonstrated performance as a key contributor to initiatives and advancement of the organization.
• Demonstrated ability to influence others without direct authority. Demonstrated ability to successfully coach / mentor in a matrixed environment. Demonstrated effective communication skills and analytical skills.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law:

• The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at thetimeofthis posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographiclocation,andwemayultimatelypaymore or less than the posted range. This range may bemodifiedin thefuture.
• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees.
• This job is eligible toparticipatein our short-term incentiveprograms.

Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.Theamountandavailabilityof anybonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employeeremainsin the Company'ssoleandabsolutediscretion unless and until paid andmay bemodifiedat the Company’s sole and absolute discretion, consistent withapplicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html